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Design, Synthesis and Biological Evaluation of Novel Catalpol Derivatives as Potential Pancreatic Cancer Inhibitors
Chemistry - An Asian Journal ( IF 3.5 ) Pub Date : 2023-05-02 , DOI: 10.1002/asia.202300185
Yuanfang Kong 1 , Shuanglin Liu 1, 2, 3 , Shaopei Wang 1, 2, 3 , Jindan Xu 1, 2, 3 , Yulong Hu 1, 2, 3 , Shiqing Jiang 1 , Chunhong Dong 1, 2, 3
Affiliation  

Catalpol isolated from Radix Rehmanniae has a variety of biological activities. A series of C10-position imidazole-modified catalpol derivatives are specifically synthesized for serving as potential pancreatic cancer inhibitors. Through molecular docking and MTT activity screening, the optimal compound was screened, which could potentially develop into anti-pancreatic cancer drug candidates.

中文翻译:


作为潜在胰腺癌抑制剂的新型梓醇衍生物的设计、合成和生物学评价



地黄中分离得到的梓醇具有多种生物活性。专门合成了一系列C10位咪唑修饰的梓醇衍生物,可作为潜在的胰腺癌抑制剂。通过分子对接和MTT活性筛选,筛选出最佳化合物,有可能开发成抗胰腺癌候选药物。
更新日期:2023-05-02
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